Longstanding effects of continuous theta burst stimulation in adult amblyopes.

Clin Exp Optom

CICS - Health Sciences Research Centre, Faculty of Health Sciences, University of Beira Interior, Covilhã, Portugal.

Published: May 2024

Clinical Relevance: Continuous theta burst stimulation may be an important tool in the therapeutic management of amblyopia, when trying to correct the established neuronal imbalance. It is important to understand whether two sessions of continuous theta burst stimulation produce greater and longstanding changes in visual acuity and suppressive imbalance than one session of continuous theta burst stimulation.

Background: We hypothesise that through the usage of continuous theta burst stimulation (cTBS) it is possible to change cortical excitability in a situation where visual impairment is present.

Methods: We selected 22 adult amblyopes, 18 females and 4 males, with an age range of 20-59 years. They were randomised into two groups: group A with 10 amblyopes was submitted to one session of cTBS and group B with 12 amblyopes submitted to two sessions of cTBS. Visual acuity (VA) and suppressive imbalance (SI) were evaluated immediately before and after stimulation in both groups A and B. A follow-up was done in both groups.

Results: For both group A and B, the VA improvements were significant after cTBS ( = 0.005 and  = 0.003, respectively). Regarding SI, both group A and B had significant improvements after cTBS ( = 0.03 and  = 0.005, respectively). Comparing groups, A and B no significant differences were found with regard to the results obtained both for VA ( = 0.72) and SI ( = 0.24). However, significant differences were found between group A and B with regard to the duration of stimulation effect for VA ( = 0.049) and SI ( = 0.03).

Conclusion: We conclude that two sessions of cTBS do not produce better results than one session of stimulation. However, it seems that two sessions of cTBS produce longstanding effects in VA and SI.

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Source
http://dx.doi.org/10.1080/08164622.2023.2228989DOI Listing

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